A new approach for the immunogenic presentation of membrane-bound human colon tumor antigens.

B H Tom, T J Goodwin, J Sengupta, B D Kahan, L P Rutzky
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引用次数: 7

Abstract

Liposomes bearing human tumor membrane vesicles were effective immunogenic complexes for inducing antibodies in rabbits. Multilamellar liposomes (MLV) at 7:4:1 molar ratios of phosphatidylcholine, cholesterol and phosphatidic acid were prepared with sonicated membrane (MN) isolated from LS174T colon tumor cells. MLV liposomes prepared together with MN (i.e., MN-MLV antigens) or MN added to preformed MLV (i.e., MN+MLV antigens), and MN antigens alone were used as immunogens. Rabbits were immunized i.v. with 100 g protein of each antigen group. Boosters (i.v.) were at days 13 and 29. Binding assays were performed by indirect radioimmunoassay on viable tumor cell targets. The MN+MLV groups were distinguished by earlier reactivity and greater specificity to the colon tumor antigens.

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膜结合人结肠肿瘤抗原免疫原性呈递的新方法。
载人肿瘤膜囊的脂质体是兔体内诱导抗体的有效免疫原性复合物。用分离自LS174T结肠肿瘤细胞的超声膜(MN)制备了磷脂酰胆碱、胆固醇和磷脂酸摩尔比为7:4:1的多层脂质体(MLV)。采用与MN(即MN-MLV抗原)共同制备的MLV脂质体,或将MN添加到预先形成的MLV(即MN+MLV抗原)中,或单独使用MN抗原作为免疫原。每组抗原蛋白100 g静脉免疫家兔。助推器(静脉注射)在第13天和第29天。结合实验采用间接放射免疫法对活的肿瘤细胞靶点进行。MN+MLV组对结肠肿瘤抗原的反应性更早,特异性更强。
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